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Found 18 with Last Name = 'arán' and Initial = 'vj'
TargetCholinesterase(Equus caballus (Horse))
Instituto De Qu£Mica M£Dica (Csic)

Curated by ChEMBL
LigandPNGBDBM50447027(CHEMBL3116284)
Affinity DataIC50:  910nMAssay Description:Inhibition of horse serum BuChE using butyrylthiocholine as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Instituto De Qu£Mica M£Dica (Csic)

Curated by ChEMBL
LigandPNGBDBM50447026(CHEMBL3116286)
Affinity DataIC50:  1.40E+3nMAssay Description:Inhibition of horse serum BuChE using butyrylthiocholine as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Instituto De Qu£Mica M£Dica (Csic)

Curated by ChEMBL
LigandPNGBDBM50447015(CHEMBL3116300)
Affinity DataIC50:  1.50E+3nMAssay Description:Inhibition of horse serum BuChE using butyrylthiocholine as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Instituto De Qu£Mica M£Dica (Csic)

Curated by ChEMBL
LigandPNGBDBM50447020(CHEMBL3116294)
Affinity DataIC50:  2.07E+3nMAssay Description:Inhibition of horse serum BuChE using butyrylthiocholine as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Instituto De Qu£Mica M£Dica (Csic)

Curated by ChEMBL
LigandPNGBDBM50447030(CHEMBL3116280)
Affinity DataIC50:  2.28E+3nMAssay Description:Inhibition of horse serum BuChE using butyrylthiocholine as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Instituto De Qu£Mica M£Dica (Csic)

Curated by ChEMBL
LigandPNGBDBM8960((+/-)-2-[(1-benzylpiperidin-4-yl)methyl]-5,6-dimet...)
Affinity DataIC50:  2.50E+3nMAssay Description:Inhibition of horse serum BuChE using butyrylthiocholine as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Instituto De Qu£Mica M£Dica (Csic)

Curated by ChEMBL
LigandPNGBDBM50447028(CHEMBL3116283)
Affinity DataIC50:  6.70E+3nMAssay Description:Inhibition of horse serum BuChE using butyrylthiocholine as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Instituto De Qu£Mica M£Dica (Csic)

Curated by ChEMBL
LigandPNGBDBM50447021(CHEMBL3116293)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of horse serum BuChE using butyrylthiocholine as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Instituto De Qu£Mica M£Dica (Csic)

Curated by ChEMBL
LigandPNGBDBM50447022(CHEMBL3116289)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of horse serum BuChE using butyrylthiocholine as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Instituto De Qu£Mica M£Dica (Csic)

Curated by ChEMBL
LigandPNGBDBM50447023(CHEMBL1973869)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of horse serum BuChE using butyrylthiocholine as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Instituto De Qu£Mica M£Dica (Csic)

Curated by ChEMBL
LigandPNGBDBM50447024(CHEMBL3116288)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of horse serum BuChE using butyrylthiocholine as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Instituto De Qu£Mica M£Dica (Csic)

Curated by ChEMBL
LigandPNGBDBM50447018(CHEMBL3116296)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of horse serum BuChE using butyrylthiocholine as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Instituto De Qu£Mica M£Dica (Csic)

Curated by ChEMBL
LigandPNGBDBM50447016(CHEMBL3116298)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of horse serum BuChE using butyrylthiocholine as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Instituto De Qu£Mica M£Dica (Csic)

Curated by ChEMBL
LigandPNGBDBM50447029(CHEMBL3116281)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of horse serum BuChE using butyrylthiocholine as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Instituto De Qu£Mica M£Dica (Csic)

Curated by ChEMBL
LigandPNGBDBM50447031(CHEMBL3116278)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of horse serum BuChE using butyrylthiocholine as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Instituto De Qu£Mica M£Dica (Csic)

Curated by ChEMBL
LigandPNGBDBM50447017(CHEMBL3116297)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of horse serum BuChE using butyrylthiocholine as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Instituto De Qu£Mica M£Dica (Csic)

Curated by ChEMBL
LigandPNGBDBM50447019(CHEMBL3116295)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of horse serum BuChE using butyrylthiocholine as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Instituto De Qu£Mica M£Dica (Csic)

Curated by ChEMBL
LigandPNGBDBM50447025(CHEMBL3116287)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of horse serum BuChE using butyrylthiocholine as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed